cheminform abstract: asymmetric propargylation of ketones using allenylboronates catalyzed by chiral...

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ChemInform 2011, 42, issue 50 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Alcohols Q 0230 DOI: 10.1002/chin.201150050 Asymmetric Propargylation of Ketones Using Allenylboronates Catalyzed by Chiral Biphenols. — Various acyclic ketones react under microwave-assisted and solvent-free conditions to afford propargylic alcohols. Ketoester (VI) and cyclic ke- tones (VIII) provide better results under conventional heating. — (BARNETT, D. S.; SCHAUS*, S. E.; Org. Lett. 13 (2011) 15, 4020-4023, http://dx.doi.org/10.1021/ol201535b ; Dep. Chem., Boston Univ., Boston, MA 02215, USA; Eng.) — R. Steudel 50- 050

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Page 1: ChemInform Abstract: Asymmetric Propargylation of Ketones Using Allenylboronates Catalyzed by Chiral Biphenols

AlcoholsQ 0230 DOI: 10.1002/chin.201150050

Asymmetric Propargylation of Ketones Using Allenylboronates Catalyzed by Chiral Biphenols. — Various acyclic ketones react under microwave-assisted and solvent-free conditions to afford propargylic alcohols. Ketoester (VI) and cyclic ke-tones (VIII) provide better results under conventional heating. — (BARNETT, D. S.; SCHAUS*, S. E.; Org. Lett. 13 (2011) 15, 4020-4023, http://dx.doi.org/10.1021/ol201535b ; Dep. Chem., Boston Univ., Boston, MA 02215, USA; Eng.) — R. Steudel

50- 050

ChemInform 2011, 42, issue 50 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim